NP-MRD: Showing NP-Card for Randioside (NP0057573)

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Record Information

Version

2.0

Created at

2022-04-28 02:59:35 UTC

Updated at

2022-04-28 02:59:35 UTC

NP-MRD ID

NP0057573

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Randioside

Description

Methyl (1S,4aR,7aR)-7-oxo-1-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,7H,7aH-cyclopenta[c]pyran-4-carboxylate belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Randioside is found in Aidia canthioides and Randia canthioides. Based on a literature review very few articles have been published on methyl (1S,4aR,7aR)-7-oxo-1-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,7H,7aH-cyclopenta[c]pyran-4-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282204592D          

 26 28  0  0  1  0            999 V2000
    0.6411   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.3646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0701    2.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    2.6021    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990    2.1896    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4990    1.3646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845    0.9521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7845    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.7541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 11  1  6  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 16 19  1  6  0  0  0
 15 20  1  1  0  0  0
 14 21  1  6  0  0  0
 21 22  1  0  0  0  0
  2 23  1  1  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
  1 26  1  6  0  0  0
M  END

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
    6.7736    0.3300   -1.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5092    0.1250   -0.7342 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5361    1.0960   -0.6778 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7897    2.2007   -1.2109 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2849    0.8614   -0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3536    1.8415   -0.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1718    1.4716    0.6548 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5085    0.2348    0.3261 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4178    0.5954   -0.6456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7311    0.4193   -0.2533 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4474    1.5877   -0.2374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5763    1.4652    0.5138 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3335    1.5025    2.0214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5707    1.3750    2.6981 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4393    0.3062    0.1484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4043    0.7147   -0.7905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7333   -0.9260   -0.2953 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3601   -1.7736    0.7264 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4625   -0.6011   -1.0928 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7725   -1.7913   -1.2390 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5435   -0.7189   -0.1213 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4142   -2.1077    0.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4575   -2.8357    0.6390 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8085   -2.5903    0.2816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6240   -1.5632    0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8408   -0.3678    0.6244 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6377    0.8706   -2.3238 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4715    0.8969   -0.7011 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2030   -0.6849   -1.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5186    2.7995   -0.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0458   -0.1356    1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6902    0.0144    0.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1979    2.3969    0.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9043    2.4664    2.3423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7528    0.6232    2.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1897    2.0763    2.3874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0067    0.0262    1.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8583   -0.0691   -1.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4338   -1.4818   -0.9843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0522   -2.4359    0.9575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7480   -0.1346   -2.0495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6108   -1.9664   -2.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7582   -0.6974   -1.2100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1412   -3.6329    0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7260   -1.6631    0.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5759   -0.1201    1.6806 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  8 21  1  0
 21 26  1  0
 26 25  1  0
 25 24  2  0
 24 22  1  0
 22 23  2  0
 26  5  1  0
 19 10  1  0
 22 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  6 30  1  0
  8 31  1  1
 10 32  1  1
 12 33  1  6
 13 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  1
 16 38  1  0
 17 39  1  6
 18 40  1  0
 19 41  1  6
 20 42  1  0
 21 43  1  6
 26 46  1  1
 25 45  1  0
 24 44  1  0
M  END


  Mrv1652304282204592D          

 26 28  0  0  1  0            999 V2000
    0.6411   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.3646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0701    2.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    2.6021    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990    2.1896    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4990    1.3646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845    0.9521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7845    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.7541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 11  1  6  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 16 19  1  6  0  0  0
 15 20  1  1  0  0  0
 14 21  1  6  0  0  0
 21 22  1  0  0  0  0
  2 23  1  1  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
  1 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0057573

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)[C@H]2[C@H]1C=CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H20O10/c1-23-14(22)7-5-24-15(10-6(7)2-3-8(10)18)26-16-13(21)12(20)11(19)9(4-17)25-16/h2-3,5-6,9-13,15-17,19-21H,4H2,1H3/t6-,9+,10-,11+,12-,13-,15-,16+/m0/s1

> <INCHI_KEY>
IKFVJCMZZBWMML-SBZOWVLFSA-N

> <FORMULA>
C16H20O10

> <MOLECULAR_WEIGHT>
372.326

> <EXACT_MASS>
372.105646844

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
34.97886690333645

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,4aR,7aR)-7-oxo-1-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <ALOGPS_LOGP>
-1.20

> <JCHEM_LOGP>
-1.548522354333333

> <ALOGPS_LOGS>
-0.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.2260945995637

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.884471174666853

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847616223457

> <JCHEM_POLAR_SURFACE_AREA>
151.98000000000002

> <JCHEM_REFRACTIVITY>
82.9617

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.92e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4aR,7aR)-7-oxo-1-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,7aH-cyclopenta[c]pyran-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.864  -0.533   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.530  -4.383   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.197  -5.153   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       3.864  -5.153   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.864  -6.693   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.530   1.777   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.864   2.547   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.864   4.087   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.198   4.857   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.531   4.087   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.531   2.547   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.198   1.777   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.198   0.237   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       7.865   1.777   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.865   4.857   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.198   6.397   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.531   7.167   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.268  -0.057   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.744   1.408   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.268  -2.549   0.000  0.00  0.00           C+0
CONECT    1    2    6   26                                                  
CONECT    2    1    3   23                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9                                                            
CONECT   11    3   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   12   18                                                  
CONECT   18   17                                                            
CONECT   19   16                                                            
CONECT   20   15                                                            
CONECT   21   14   22                                                       
CONECT   22   21                                                            
CONECT   23    2   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25    1                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,4ar,7ar)-7-oxo-1-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4ah,7H,7ah-cyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₁₆H₂₀O₁₀

Average Mass

372.3260 Da

Monoisotopic Mass

372.10565 Da

IUPAC Name

methyl (1S,4aR,7aR)-7-oxo-1-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,7H,7aH-cyclopenta[c]pyran-4-carboxylate

Traditional Name

methyl (1S,4aR,7aR)-7-oxo-1-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,7aH-cyclopenta[c]pyran-4-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)[C@H]2[C@H]1C=CC2=O

InChI Identifier

InChI=1S/C16H20O10/c1-23-14(22)7-5-24-15(10-6(7)2-3-8(10)18)26-16-13(21)12(20)11(19)9(4-17)25-16/h2-3,5-6,9-13,15-17,19-21H,4H2,1H3/t6-,9+,10-,11+,12-,13-,15-,16+/m0/s1

InChI Key

IKFVJCMZZBWMML-SBZOWVLFSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Aidia canthioides	LOTUS Database	35616633
Randia canthioides	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
O-glycosyl compound
Oxane
Monosaccharide
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
Primary alcohol
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-1.2	ALOGPS
logP	-1.5	ChemAxon
logS	-0.98	ALOGPS
pKa (Strongest Acidic)	10.88	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.98 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	82.96 m³·mol⁻¹	ChemAxon
Polarizability	34.98 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162934885

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Randioside (NP0057573)

MOL for NP0057573 (Randioside)

3D MOL for NP0057573 (Randioside)

3D SDF for NP0057573 (Randioside)

3D-SDF for NP0057573 (Randioside)

PDB for NP0057573 (Randioside)

3D PDB for NP0057573 (Randioside)

SMILES for NP0057573 (Randioside)

INCHI for NP0057573 (Randioside)

Structure for NP0057573 (Randioside)

3D Structure for NP0057573 (Randioside)